Job Description

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.

Responsibilities:        

• Under limited supervision, perform equipment setup, operation, troubleshoot to meet all
  standards for safety, quality and efficiency.
• Maintain machine uptime, perform any fault clearing and clear stoppages on automated
  equipment.
• Perform basic, routine manufacturing process operations such as dispensing of raw
  materials, material reconciliation, line clearance, basic analytics, and record transactions
• Assist in the review of documentation for assigned areas (i.e. procedures, job plans, logs,
  area audits and batch records)
• Assist as training resource on manufacturing tasks and equipment use
• Use human machine interfaces (HMIs) to identify alarms and correct line stoppages.
• Ensures components and products are available for a continuous operation.
• Troubleshoot and identify potential solutions for mechanical errors, safety issues or general
  operating inefficiencies within the production processes.
• Partner with cross-functional teams to help drive improvement opportunities.
• Safely follow standardized operating procedures including material handling, record keeping,
  assembly and packaging. Must follow Good Manufacturing Practices (GMPs).
• Train fellow staff on the manufacturing processes, equipment, and general skills

Qualifications:

• High school/GED + 2 years' work experience OR​ Associates and 6 months' work experience OR​ Bachelors
• Operations and Manufacturing experience
• Ability to work in teams
• Understand Good Manufacturing Practices
• Ability to operate equipment, documentation and train other operators
• Able to use computer systems to support material inventory system (SAP transactions) and
  electronic batch records.
• 2nd shift 230pm -1130pm M-F Until Oct 2025, then schedule with transfer into a AM shift 6am-630pm 3days a week and every other weekend.

Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity,, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.

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